Canonical Allele Identifier: CA913169908

Gene:

Linked Data

• ClinVar Variation Id: 690179
• ClinVar RCV Id: RCV000851066
• dbSNP Id: rs1603223643

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12265A>G , J01415.2:m.12265A>G	GRCh38